Abstract
The 70-kDa peroxisomal membrane protein (PXMP1) is a member of the ATP-binding cassette transporter family. In humans) mutations in this gene may be responsible for a subset of patients with Zellweger syndrome, a lethal inborn error of peroxisome assembly. The PXMP1 gene was assigned to human chromosome 1p21-p22 by in situ hybridization and its murine homologue (Pxmp-1) to chromosome 3 by interspecific backcross analysis.
Original language | English (US) |
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Pages (from-to) | 412-414 |
Number of pages | 3 |
Journal | Genomics |
Volume | 15 |
Issue number | 2 |
DOIs | |
State | Published - Feb 1993 |
ASJC Scopus subject areas
- Genetics